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Lactic acid cream can help improve skin bumps known as eruptive vellus hair cysts.

A peptide called DPS-1 helps human scalp cells grow and stimulates hair growth in mice.

A patient with Cronkhite-Canada Syndrome developed colon cancer that spread to the liver, showing the need for regular cancer checks in such patients.

Congenital atrichia is a rare condition where children are born without hair, and treatment is often ineffective.

Children's hair loss can be caused by various factors and should be treated with appropriate, age-specific methods and psychological support.

The document concludes that non-endocrine alopecia in pets varies in treatment effectiveness and often has a poor prognosis, especially in cats.

Bovines can have rare inherited skin diseases with specific symptoms like hair loss, fragile skin, and abnormal porphyrin buildup.

Changing hair follicle identity could potentially reverse balding.

A new medical syndrome may include skin changes, hair loss, sweating issues, bone malformations, leg swelling, and low cortisol.

About 30% of women feel they lose too much hair, often starting before age 40, and most can't find a reason for it.

Understanding gene expression in hair follicles can reveal insights into hair growth and disorders.

Different types of stem cells in hair follicles play unique roles in wound healing and hair growth, with some stem cells not originating from existing hair follicles but from non-hair follicle cells. WNT signaling and the Lhx2 factor are key in creating new hair follicles.

Scientists created stem cells that can grow hair and skin.

Trichoscopy is a useful non-invasive method for diagnosing different hair loss conditions.

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

The study found that Keratosis Pilaris Atrophicans is a genetic skin condition that starts in childhood, involves inflammation and scarring, and current treatments are only somewhat effective.

The guide explains how to identify and treat children's hair loss, including fungal infections, autoimmune disorders, hairstyle changes, self-correcting conditions, and behavioral therapy for hair-pulling.

Some children are born with unusually short, fine hair because their hair growth phase is short, but this often gets better by itself during puberty.

The study concludes that the EDA2R gene is activated by p53 during chemotherapy but is not necessary for chemotherapy-induced hair loss.

Loose anagen hair syndrome is caused by structural abnormalities in the hair follicle's inner root sheath.

Some families have a genetic condition where they are born with irregular scalp defects.

Loose Anagen Syndrome causes easy-to-pull, thin hair, mainly in young girls, and improves with age.

DNA methylation and long non-coding RNAs are key in controlling hair growth in Cashmere goats.

Blocking the FGF5 gene in sheep leads to more fine wool and active hair follicles due to changes in certain cell signaling pathways.

Stem cell differentiation is crucial for skin barrier maintenance and its disruption can lead to skin diseases.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

The Notch signaling pathway helps in mouse hair development through a noncanonical mechanism that does not rely on RBPj or transcription.

Leg hair can be used for eyelash transplants, resulting in fuller lashes with less maintenance.

Four children had unmanageable pale blond hair due to uncombable-hair syndrome.

White piedra, a rare fungal infection, was diagnosed in two women in a northern climate.